ID: ALA447806

Max Phase: Preclinical

Molecular Formula: C19H23N3O4

Molecular Weight: 357.41

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(CCCCCC(=O)NN/C=C/c1c(O)ccc2ccccc12)NO

Standard InChI:  InChI=1S/C19H23N3O4/c23-17-11-10-14-6-4-5-7-15(14)16(17)12-13-20-21-18(24)8-2-1-3-9-19(25)22-26/h4-7,10-13,20,23,26H,1-3,8-9H2,(H,21,24)(H,22,25)/b13-12+

Standard InChI Key:  MJRUMFRGCVBFFS-OUKQBFOZSA-N

Associated Targets(Human)

MM1.S 1111 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Histone deacetylase 41 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 357.41Molecular Weight (Monoisotopic): 357.1689AlogP: 2.59#Rotatable Bonds: 9
Polar Surface Area: 110.69Molecular Species: NEUTRALHBA: 5HBD: 5
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.68CX Basic pKa: 1.27CX LogP: 2.04CX LogD: 2.02
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.27Np Likeness Score: -0.21

References

1. Patel V, Mazitschek R, Coleman B, Nguyen C, Urgaonkar S, Cortese J, Barker RH, Greenberg E, Tang W, Bradner JE, Schreiber SL, Duraisingh MT, Wirth DF, Clardy J..  (2009)  Identification and characterization of small molecule inhibitors of a class I histone deacetylase from Plasmodium falciparum.,  52  (8): [PMID:19317450] [10.1021/jm801654y]

Source